PSYCHOMETRIC DEVIANCE IN OFFSPRING AT RISK FOR SCHIZOPHRENIA .2. RESOLVING HETEROGENEITY THROUGH ADMIXTURE ANALYSIS

被引:24
作者
MOLDIN, SO
RICE, JP
GOTTESMAN, II
ERLENMEYERKIMLING, L
机构
[1] WASHINGTON UNIV, SCH MED, ST LOUIS, MO 63110 USA
[2] UNIV VIRGINIA, CHARLOTTESVILLE, VA 22903 USA
[3] COLUMBIA UNIV COLL PHYS & SURG, NEW YORK, NY 10032 USA
[4] NEW YORK STATE PSYCHIAT INST & HOSP, DEPT MED GENET, DIV DEV BEHAV STUDIES, NEW YORK, NY 10032 USA
关键词
admixture (commingling); bimodality; heterogeneity; high-risk studies; indicators of liability; Minnesota Multiphasic Personality Inventory; Schizophrenia;
D O I
10.1016/0165-1781(90)90036-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The longitudinal and prospective study of offspring at risk for schizophrenia is complicated by within-group heterogeneity in liability, as only a subgroup of those at risk will ultimately become affected. Here, we attempt to resolve such heterogeneity in the New York High-Risk Project by conducting an admixture analysis of values on a psychometric index of liability to schizophrenia derived from the Minnesota Multiphasic Personality Inventory (MMPI). We fit mixtures of components to the overall distribution in 171 children from three criterion groups: offspring at risk (HR) for schizophrenia, psychiatric comparison (PC) offspring at risk for affective illness, and normal comparison (NC) offspring not at increased risk for psychiatric morbidity. The distribution of psychometric scores was bimodal, and separation of two latent classes showed that there is a valid and nonarbitrary distinction between a subgroup of MMPI-deviant (primarily HR) offspring and a larger homogeneous group of MMPI-nondeviant HR, PC, and NC subjects. While continued followup is required to demonstrate a correspondence between these two classes and an underlying taxonomy of liability to schizophrenia, our findings demonstrate the utility of objective psychometric measurement and admixture analysis for resolving within-group heterogeneity in high-risk research. The wider implications of including our MMPI indicators in other genetic investigations of schizophrenia are discussed. © 1990.
引用
收藏
页码:311 / 322
页数:12
相关论文
共 47 条
[11]  
ERLENMEYERKIMLI.L, 1987, BIOL PERSPECTIVES SC, P33
[12]  
ERLENMEYERKIMLI.L, 1978, NATURE SCHIZOPHRENIA, P359
[13]  
ERLENMEYERKIMLI.L, 1968, TRANSMISSION SCHIZOP, P65
[14]   THE NEW-YORK-HIGH-RISK-PROJECT - A FOLLOW-UP REPORT [J].
ERLENMEYERKIMLING, L ;
CORNBLATT, B .
SCHIZOPHRENIA BULLETIN, 1987, 13 (03) :451-461
[15]   HIGH-RISK RESEARCH IN SCHIZOPHRENIA - A SUMMARY OF WHAT HAS BEEN LEARNED [J].
ERLENMEYERKIMLING, L ;
CORNBLATT, B .
JOURNAL OF PSYCHIATRIC RESEARCH, 1987, 21 (04) :401-411
[16]  
GIBBONS RD, 1984, BIOL PSYCHIAT, V19, P935
[17]   DETECTION OF THE SCHIZOID TAXON WITH MMPI INDICATORS [J].
GOLDEN, RR ;
MEEHL, PE .
JOURNAL OF ABNORMAL PSYCHOLOGY, 1979, 88 (03) :217-233
[18]  
Gottesman I.I., 1982, SCHIZOPHRENIA EPIGEN
[19]  
GOTTESMAN II, 1989, ARCH GEN PSYCHIAT, V46, P867
[20]   GENETIC THEORIES AND VALIDATION OF PSYCHIATRIC DIAGNOSES - IMPLICATIONS FOR STUDY OF CHILDREN OF SCHIZOPHRENICS [J].
HANSON, DR ;
GOTTESMAN, II ;
MEEHL, PE .
JOURNAL OF ABNORMAL PSYCHOLOGY, 1977, 86 (06) :575-588